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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 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: A0A3S7X2J5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.668 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 516 | 522 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.524 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.496 |
DEG_APCC_DBOX_1 | 374 | 382 | PF00400 | 0.463 |
DEG_ODPH_VHL_1 | 385 | 397 | PF01847 | 0.439 |
DEG_SCF_FBW7_1 | 474 | 479 | PF00400 | 0.576 |
DOC_ANK_TNKS_1 | 265 | 272 | PF00023 | 0.457 |
DOC_CKS1_1 | 182 | 187 | PF01111 | 0.606 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.588 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.564 |
DOC_MAPK_gen_1 | 138 | 144 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 191 | 199 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 221 | 229 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 221 | 229 | PF00069 | 0.441 |
DOC_MAPK_NFAT4_5 | 139 | 147 | PF00069 | 0.395 |
DOC_MAPK_NFAT4_5 | 222 | 230 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 532 | 539 | PF00149 | 0.570 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.518 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 274 | 283 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 367 | 374 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 415 | 423 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 462 | 469 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 66 | 73 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.809 |
LIG_Actin_WH2_2 | 366 | 384 | PF00022 | 0.431 |
LIG_AP2alpha_1 | 209 | 213 | PF02296 | 0.482 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.526 |
LIG_APCC_ABBA_1 | 254 | 259 | PF00400 | 0.375 |
LIG_APCC_ABBA_1 | 506 | 511 | PF00400 | 0.508 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.630 |
LIG_BIR_III_4 | 334 | 338 | PF00653 | 0.620 |
LIG_deltaCOP1_diTrp_1 | 112 | 121 | PF00928 | 0.497 |
LIG_deltaCOP1_diTrp_1 | 161 | 170 | PF00928 | 0.601 |
LIG_EVH1_2 | 246 | 250 | PF00568 | 0.368 |
LIG_EVH1_2 | 393 | 397 | PF00568 | 0.483 |
LIG_EVH1_2 | 43 | 47 | PF00568 | 0.567 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.640 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.360 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.324 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.643 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.747 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.605 |
LIG_Integrin_RGD_1 | 215 | 217 | PF01839 | 0.485 |
LIG_LIR_Gen_1 | 112 | 119 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 420 | 431 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.540 |
LIG_NRBOX | 224 | 230 | PF00104 | 0.439 |
LIG_NRP_CendR_1 | 537 | 539 | PF00754 | 0.597 |
LIG_Pex14_2 | 209 | 213 | PF04695 | 0.536 |
LIG_PTB_Apo_2 | 444 | 451 | PF02174 | 0.409 |
LIG_PTB_Phospho_1 | 444 | 450 | PF10480 | 0.407 |
LIG_SH2_GRB2like | 445 | 448 | PF00017 | 0.400 |
LIG_SH2_GRB2like | 486 | 489 | PF00017 | 0.534 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.559 |
LIG_SH2_SRC | 445 | 448 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.649 |
LIG_SH3_1 | 525 | 531 | PF00018 | 0.550 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.674 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.396 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.355 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.527 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.578 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.602 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.761 |
LIG_SH3_CIN85_PxpxPR_1 | 94 | 99 | PF14604 | 0.594 |
LIG_SUMO_SIM_anti_2 | 315 | 322 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 315 | 322 | PF11976 | 0.408 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.472 |
LIG_UBA3_1 | 227 | 233 | PF00899 | 0.424 |
MOD_CDK_SPK_2 | 11 | 16 | PF00069 | 0.510 |
MOD_CDK_SPK_2 | 86 | 91 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 527 | 534 | PF00069 | 0.578 |
MOD_CDK_SPxxK_3 | 84 | 91 | PF00069 | 0.643 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.656 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.510 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.577 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.339 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.530 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.823 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.565 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.539 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.662 |
MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.435 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.517 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.368 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.518 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.614 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.594 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.645 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.509 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.560 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.529 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.443 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.476 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.492 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.729 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.554 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.439 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.628 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.719 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.652 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.594 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.626 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.366 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.610 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.512 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.391 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.624 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.677 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.601 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.611 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.534 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.509 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.551 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.510 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.579 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.421 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.483 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.570 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.546 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.655 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.629 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.618 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 412 | 417 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 310 | 315 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 415 | 420 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 467 | 472 | PF00026 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P950 | Leptomonas seymouri | 39% | 96% |
A0A3Q8IAB6 | Leishmania donovani | 26% | 100% |
A0A3R7KFA4 | Trypanosoma rangeli | 31% | 100% |
A4H889 | Leishmania braziliensis | 26% | 100% |
A4HHF5 | Leishmania braziliensis | 81% | 100% |
A4HWL2 | Leishmania infantum | 26% | 100% |
A4I4K3 | Leishmania infantum | 100% | 100% |
C9ZL87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AE02 | Leishmania major | 94% | 100% |
E9ALT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AQB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4QF55 | Leishmania major | 25% | 100% |