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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X0H0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.402 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.643 |
CLV_PCSK_FUR_1 | 271 | 275 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.647 |
CLV_Separin_Metazoa | 536 | 540 | PF03568 | 0.738 |
DOC_CKS1_1 | 401 | 406 | PF01111 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 136 | 142 | PF00134 | 0.645 |
DOC_CYCLIN_yCln2_LP_2 | 443 | 449 | PF00134 | 0.656 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.598 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 539 | 549 | PF00069 | 0.774 |
DOC_MAPK_gen_1 | 568 | 574 | PF00069 | 0.609 |
DOC_MAPK_gen_1 | 87 | 94 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 22 | 30 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.552 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 136 | 139 | PF13499 | 0.595 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.613 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 401 | 404 | PF00568 | 0.541 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.635 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 242 | 250 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 297 | 301 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 470 | 479 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.601 |
LIG_AP2alpha_1 | 63 | 67 | PF02296 | 0.629 |
LIG_AP2alpha_2 | 300 | 302 | PF02296 | 0.609 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.580 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.517 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.527 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.473 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.523 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.571 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.566 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.576 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.736 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.555 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.483 |
LIG_LIR_Apic_2 | 398 | 404 | PF02991 | 0.556 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.534 |
LIG_PDZ_Class_1 | 594 | 599 | PF00595 | 0.649 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.629 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.441 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.501 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.336 |
LIG_SH2_SRC | 261 | 264 | PF00017 | 0.563 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.576 |
LIG_SH2_SRC | 311 | 314 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.658 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.574 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.534 |
LIG_SH3_2 | 263 | 268 | PF14604 | 0.570 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.466 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.549 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.580 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.606 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.623 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 348 | 353 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.557 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.464 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.642 |
LIG_TYR_ITSM | 398 | 405 | PF00017 | 0.524 |
MOD_CDC14_SPxK_1 | 376 | 379 | PF00782 | 0.747 |
MOD_CDK_SPxK_1 | 373 | 379 | PF00069 | 0.777 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.566 |
MOD_CDK_SPxK_1 | 540 | 546 | PF00069 | 0.626 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.759 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.692 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.483 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.669 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.495 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.762 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.622 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.628 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.567 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.490 |
MOD_Cter_Amidation | 194 | 197 | PF01082 | 0.739 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.504 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.520 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.764 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.522 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.450 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.669 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.641 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.560 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.729 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.764 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.773 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.776 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.509 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.723 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.665 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.594 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.497 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.658 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.712 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.640 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.641 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.645 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.710 |
MOD_N-GLC_2 | 370 | 372 | PF02516 | 0.721 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.636 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.651 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.577 |
MOD_PK_1 | 409 | 415 | PF00069 | 0.454 |
MOD_PKA_1 | 196 | 202 | PF00069 | 0.710 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.567 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.683 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.377 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.596 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.771 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.729 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.578 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.674 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.587 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.529 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.540 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.583 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.512 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.599 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.502 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.566 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.634 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.599 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.694 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.777 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.570 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.596 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.664 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.474 |
MOD_SUMO_rev_2 | 252 | 256 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 353 | 361 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 525 | 535 | PF00179 | 0.783 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.583 |
TRG_DiLeu_LyEn_5 | 165 | 170 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 491 | 494 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I592 | Leptomonas seymouri | 54% | 97% |
A0A1X0P512 | Trypanosomatidae | 36% | 100% |
A0A422NTD4 | Trypanosoma rangeli | 37% | 100% |
A4HFH4 | Leishmania braziliensis | 74% | 100% |
A4I2N4 | Leishmania infantum | 100% | 100% |
D0A5Q0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AD25 | Leishmania major | 91% | 100% |
E9AYV0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BSP9 | Trypanosoma cruzi | 36% | 100% |