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: A0A3Q8IE56
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 | 0.710 |
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.337 |
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.393 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.506 |
CLV_PCSK_FUR_1 | 578 | 582 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.444 |
DEG_APCC_DBOX_1 | 508 | 516 | PF00400 | 0.400 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.620 |
DEG_SPOP_SBC_1 | 236 | 240 | PF00917 | 0.619 |
DOC_CDC14_PxL_1 | 60 | 68 | PF14671 | 0.588 |
DOC_CKS1_1 | 447 | 452 | PF01111 | 0.281 |
DOC_MAPK_gen_1 | 280 | 290 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 423 | 429 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 578 | 588 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 280 | 288 | PF00069 | 0.314 |
DOC_MIT_MIM_1 | 300 | 310 | PF04212 | 0.360 |
DOC_PP1_RVXF_1 | 423 | 430 | PF00149 | 0.281 |
DOC_PP1_RVXF_1 | 512 | 519 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.266 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.593 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.300 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.411 |
DOC_USP7_MATH_2 | 265 | 271 | PF00917 | 0.505 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.728 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 401 | 407 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 585 | 589 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.444 |
LIG_AP2alpha_1 | 277 | 281 | PF02296 | 0.393 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.633 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.580 |
LIG_BRCT_BRCA1_1 | 592 | 596 | PF00533 | 0.512 |
LIG_CtBP_PxDLS_1 | 450 | 454 | PF00389 | 0.281 |
LIG_deltaCOP1_diTrp_1 | 296 | 300 | PF00928 | 0.360 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.600 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.587 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.333 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.285 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.268 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.645 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.652 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.515 |
LIG_LIR_Apic_2 | 279 | 284 | PF02991 | 0.325 |
LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 367 | 373 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 22 | 33 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 47 | 58 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 74 | 85 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.339 |
LIG_PCNA_yPIPBox_3 | 329 | 341 | PF02747 | 0.373 |
LIG_PDZ_Class_2 | 595 | 600 | PF00595 | 0.514 |
LIG_Pex14_1 | 456 | 460 | PF04695 | 0.325 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.418 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.281 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.266 |
LIG_Pex14_2 | 548 | 552 | PF04695 | 0.351 |
LIG_Pex14_2 | 596 | 600 | PF04695 | 0.519 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.331 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 412 | 415 | PF00017 | 0.300 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.281 |
LIG_SH2_PTP2 | 112 | 115 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 77 | 80 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.281 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.328 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.747 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.300 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.369 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.393 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.305 |
LIG_SUMO_SIM_par_1 | 286 | 292 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.284 |
LIG_TRAF2_1 | 536 | 539 | PF00917 | 0.531 |
LIG_TRFH_1 | 189 | 193 | PF08558 | 0.452 |
LIG_WRC_WIRS_1 | 28 | 33 | PF05994 | 0.439 |
LIG_WW_1 | 186 | 189 | PF00397 | 0.582 |
MOD_CDC14_SPxK_1 | 326 | 329 | PF00782 | 0.331 |
MOD_CDK_SPK_2 | 253 | 258 | PF00069 | 0.730 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.637 |
MOD_CDK_SPxK_1 | 323 | 329 | PF00069 | 0.411 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.639 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.699 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.732 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.658 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.378 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.572 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.331 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.461 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.783 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.753 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.383 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.266 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.531 |
MOD_Cter_Amidation | 421 | 424 | PF01082 | 0.281 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.534 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.704 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.727 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.395 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.484 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.368 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.403 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.386 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.494 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.453 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.640 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.549 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.686 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.617 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.303 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.441 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.620 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.266 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.608 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.566 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.443 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.664 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.266 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.266 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.433 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.784 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.393 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.266 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.386 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.463 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.637 |
MOD_OFUCOSY | 67 | 73 | PF10250 | 0.476 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.266 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.712 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.331 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.456 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.384 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.373 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.626 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.442 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.272 |
MOD_Plk_2-3 | 359 | 365 | PF00069 | 0.403 |
MOD_Plk_2-3 | 534 | 540 | PF00069 | 0.543 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.447 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.469 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.316 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.621 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.554 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.722 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.645 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.525 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.577 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.640 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.594 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.408 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.325 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.281 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.505 |
MOD_SUMO_rev_2 | 138 | 145 | PF00179 | 0.765 |
TRG_AP2beta_CARGO_1 | 379 | 389 | PF09066 | 0.300 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 543 | 546 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.570 |
TRG_ER_FFAT_2 | 379 | 387 | PF00635 | 0.210 |
TRG_NES_CRM1_1 | 52 | 65 | PF08389 | 0.494 |
TRG_NLS_MonoExtC_3 | 134 | 139 | PF00514 | 0.632 |
TRG_NLS_MonoExtN_4 | 133 | 140 | PF00514 | 0.697 |
TRG_NLS_MonoExtN_4 | 223 | 229 | PF00514 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 569 | 573 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4D1 | Leptomonas seymouri | 74% | 100% |
A0A0S4JT19 | Bodo saltans | 46% | 100% |
A0A1X0P469 | Trypanosomatidae | 51% | 100% |
A0A422NFR7 | Trypanosoma rangeli | 51% | 100% |
A4HFQ9 | Leishmania braziliensis | 85% | 99% |
A4I2T5 | Leishmania infantum | 100% | 100% |
D0A601 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ADB3 | Leishmania major | 94% | 100% |
E9AZ38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BL30 | Trypanosoma cruzi | 51% | 100% |