Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZ38
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018195 | peptidyl-arginine modification | 6 | 1 |
GO:0018216 | peptidyl-arginine methylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034969 | histone arginine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0043985 | histone H4-R3 methylation | 7 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000976 | transcription cis-regulatory region binding | 5 | 1 |
GO:0000987 | cis-regulatory region sequence-specific DNA binding | 6 | 1 |
GO:0001067 | transcription regulatory region nucleic acid binding | 4 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 1 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.285 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 578 | 582 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.434 |
DEG_APCC_DBOX_1 | 508 | 516 | PF00400 | 0.404 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.550 |
DEG_SCF_FBW7_2 | 149 | 154 | PF00400 | 0.446 |
DEG_SPOP_SBC_1 | 235 | 239 | PF00917 | 0.636 |
DOC_CDC14_PxL_1 | 60 | 68 | PF14671 | 0.553 |
DOC_CKS1_1 | 447 | 452 | PF01111 | 0.286 |
DOC_MAPK_gen_1 | 280 | 290 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 423 | 429 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 578 | 588 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 280 | 288 | PF00069 | 0.336 |
DOC_MIT_MIM_1 | 300 | 310 | PF04212 | 0.365 |
DOC_PP1_RVXF_1 | 423 | 430 | PF00149 | 0.286 |
DOC_PP1_RVXF_1 | 512 | 519 | PF00149 | 0.383 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.271 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.550 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.306 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.415 |
DOC_USP7_MATH_2 | 198 | 204 | PF00917 | 0.459 |
DOC_USP7_MATH_2 | 265 | 271 | PF00917 | 0.492 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.713 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 268 | 274 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 401 | 407 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 585 | 589 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.418 |
LIG_AP2alpha_1 | 277 | 281 | PF02296 | 0.398 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 592 | 596 | PF00533 | 0.516 |
LIG_CtBP_PxDLS_1 | 450 | 454 | PF00389 | 0.286 |
LIG_deltaCOP1_diTrp_1 | 296 | 300 | PF00928 | 0.365 |
LIG_EVH1_2 | 155 | 159 | PF00568 | 0.437 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.573 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.325 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.290 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.267 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.644 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.358 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.630 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.614 |
LIG_LIR_Apic_2 | 279 | 284 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 367 | 373 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 22 | 33 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 47 | 58 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 74 | 85 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.313 |
LIG_PDZ_Class_2 | 595 | 600 | PF00595 | 0.515 |
LIG_Pex14_1 | 456 | 460 | PF04695 | 0.331 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.401 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.286 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.271 |
LIG_Pex14_2 | 548 | 552 | PF04695 | 0.351 |
LIG_Pex14_2 | 596 | 600 | PF04695 | 0.519 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.343 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.495 |
LIG_SH2_GRB2like | 412 | 415 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.286 |
LIG_SH2_PTP2 | 112 | 115 | PF00017 | 0.477 |
LIG_SH2_PTP2 | 77 | 80 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.297 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.447 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.750 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.328 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.374 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.398 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.286 |
LIG_SUMO_SIM_par_1 | 286 | 292 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.289 |
LIG_TRAF2_1 | 464 | 467 | PF00917 | 0.385 |
LIG_TRAF2_1 | 536 | 539 | PF00917 | 0.526 |
LIG_TRFH_1 | 189 | 193 | PF08558 | 0.392 |
LIG_WW_1 | 186 | 189 | PF00397 | 0.481 |
MOD_CDC14_SPxK_1 | 326 | 329 | PF00782 | 0.343 |
MOD_CDK_SPK_2 | 253 | 258 | PF00069 | 0.715 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.641 |
MOD_CDK_SPxK_1 | 323 | 329 | PF00069 | 0.415 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.640 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.688 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.728 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.661 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.368 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.577 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.343 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.441 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.766 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.758 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.369 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.271 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.271 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.514 |
MOD_Cter_Amidation | 421 | 424 | PF01082 | 0.286 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.731 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.627 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.816 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.514 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.437 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.364 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.378 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.502 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.433 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.645 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.537 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.704 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.551 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.644 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.306 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.418 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.622 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.271 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.609 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.566 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.406 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.662 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.271 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.271 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.413 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.472 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.725 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.429 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.349 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.271 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.369 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.358 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.453 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.627 |
MOD_OFUCOSY | 67 | 73 | PF10250 | 0.439 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.271 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.698 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.343 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.435 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.382 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.647 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.405 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.232 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.252 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.310 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.478 |
MOD_Plk_2-3 | 331 | 337 | PF00069 | 0.227 |
MOD_Plk_2-3 | 534 | 540 | PF00069 | 0.535 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.337 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.472 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.483 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.343 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.616 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.525 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.711 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.641 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.426 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.558 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.584 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.371 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.311 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.209 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.483 |
MOD_SUMO_rev_2 | 138 | 145 | PF00179 | 0.753 |
TRG_AP2beta_CARGO_1 | 379 | 389 | PF09066 | 0.306 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 543 | 546 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.567 |
TRG_NES_CRM1_1 | 52 | 65 | PF08389 | 0.483 |
TRG_NLS_MonoExtC_3 | 134 | 139 | PF00514 | 0.620 |
TRG_NLS_MonoExtC_3 | 224 | 230 | PF00514 | 0.571 |
TRG_NLS_MonoExtN_4 | 133 | 140 | PF00514 | 0.685 |
TRG_NLS_MonoExtN_4 | 223 | 229 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 569 | 573 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4D1 | Leptomonas seymouri | 74% | 100% |
A0A0S4JT19 | Bodo saltans | 45% | 100% |
A0A1X0P469 | Trypanosomatidae | 51% | 100% |
A0A3Q8IE56 | Leishmania donovani | 94% | 100% |
A0A422NFR7 | Trypanosoma rangeli | 51% | 100% |
A4HFQ9 | Leishmania braziliensis | 85% | 99% |
A4I2T5 | Leishmania infantum | 94% | 100% |
D0A601 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ADB3 | Leishmania major | 94% | 100% |
V5BL30 | Trypanosoma cruzi | 50% | 100% |