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: A4HFQ9
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 | 226 | 230 | PF00656 | 0.735 |
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.736 |
CLV_C14_Caspase3-7 | 306 | 310 | PF00656 | 0.285 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.485 |
CLV_PCSK_FUR_1 | 572 | 576 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.694 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.514 |
CLV_PCSK_PC7_1 | 258 | 264 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.486 |
DEG_APCC_DBOX_1 | 502 | 510 | PF00400 | 0.423 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.618 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.615 |
DEG_SPOP_SBC_1 | 527 | 531 | PF00917 | 0.399 |
DOC_CDC14_PxL_1 | 60 | 68 | PF14671 | 0.582 |
DOC_CKS1_1 | 441 | 446 | PF01111 | 0.286 |
DOC_MAPK_gen_1 | 262 | 268 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 417 | 423 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 572 | 582 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 277 | 284 | PF00069 | 0.337 |
DOC_MIT_MIM_1 | 294 | 304 | PF04212 | 0.365 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.286 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.271 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.588 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.306 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.492 |
DOC_USP7_MATH_2 | 259 | 265 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 145 | 151 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 224 | 232 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 362 | 367 | PF00244 | 0.192 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.439 |
LIG_BIR_III_2 | 121 | 125 | PF00653 | 0.480 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.589 |
LIG_BRCT_BRCA1_1 | 586 | 590 | PF00533 | 0.522 |
LIG_Clathr_ClatBox_1 | 580 | 584 | PF01394 | 0.415 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.286 |
LIG_deltaCOP1_diTrp_1 | 290 | 294 | PF00928 | 0.365 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.577 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.588 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.325 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.290 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.260 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.493 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.607 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.661 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.192 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.645 |
LIG_LIR_Apic_2 | 273 | 278 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 3 | 7 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 361 | 367 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 22 | 33 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 373 | 384 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 47 | 58 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 74 | 85 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.329 |
LIG_PCNA_yPIPBox_3 | 323 | 335 | PF02747 | 0.378 |
LIG_PDZ_Class_2 | 589 | 594 | PF00595 | 0.516 |
LIG_Pex14_1 | 450 | 454 | PF04695 | 0.331 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.408 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.286 |
LIG_Pex14_2 | 350 | 354 | PF04695 | 0.271 |
LIG_Pex14_2 | 542 | 546 | PF04695 | 0.351 |
LIG_Pex14_2 | 590 | 594 | PF04695 | 0.521 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.343 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 406 | 409 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 364 | 368 | PF00017 | 0.286 |
LIG_SH2_PTP2 | 77 | 80 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.311 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.328 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.374 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.286 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.394 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 29 | 36 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.192 |
LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.289 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.385 |
LIG_TRAF2_1 | 530 | 533 | PF00917 | 0.539 |
LIG_WW_1 | 185 | 188 | PF00397 | 0.512 |
MOD_CDC14_SPxK_1 | 320 | 323 | PF00782 | 0.343 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.653 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.415 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.654 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.706 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.371 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.587 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.343 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.455 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.781 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.475 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.372 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.271 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.271 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.530 |
MOD_Cter_Amidation | 142 | 145 | PF01082 | 0.630 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.586 |
MOD_Cter_Amidation | 415 | 418 | PF01082 | 0.286 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.712 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.437 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.364 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.407 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.391 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.448 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.642 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.559 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.662 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.631 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.306 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.608 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.418 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.271 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.622 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.426 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.271 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.271 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.426 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.711 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.429 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.546 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.271 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.390 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.566 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.472 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.635 |
MOD_OFUCOSY | 67 | 73 | PF10250 | 0.460 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.556 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.465 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.271 |
MOD_PKA_1 | 307 | 313 | PF00069 | 0.343 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.449 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.694 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.391 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.378 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.426 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.252 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.310 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.407 |
MOD_Plk_2-3 | 528 | 534 | PF00069 | 0.549 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.466 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.375 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.493 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.343 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.299 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.361 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.548 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.654 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.635 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.557 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.579 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.371 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.311 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.209 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.502 |
TRG_AP2beta_CARGO_1 | 373 | 383 | PF09066 | 0.306 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 417 | 420 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 52 | 65 | PF08389 | 0.501 |
TRG_NLS_MonoExtC_3 | 134 | 140 | PF00514 | 0.632 |
TRG_NLS_MonoExtN_4 | 133 | 139 | PF00514 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 563 | 567 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4D1 | Leptomonas seymouri | 73% | 99% |
A0A0S4JT19 | Bodo saltans | 44% | 100% |
A0A1X0P469 | Trypanosomatidae | 50% | 100% |
A0A3Q8IE56 | Leishmania donovani | 85% | 99% |
A0A422NFR7 | Trypanosoma rangeli | 52% | 100% |
A4I2T5 | Leishmania infantum | 84% | 99% |
D0A601 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ADB3 | Leishmania major | 84% | 100% |
E9AZ38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
V5BL30 | Trypanosoma cruzi | 50% | 100% |