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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4HG38
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 499 | 503 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.727 |
CLV_PCSK_FUR_1 | 161 | 165 | PF00082 | 0.424 |
CLV_PCSK_FUR_1 | 170 | 174 | PF00082 | 0.476 |
CLV_PCSK_FUR_1 | 270 | 274 | PF00082 | 0.432 |
CLV_PCSK_FUR_1 | 279 | 283 | PF00082 | 0.484 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.427 |
CLV_PCSK_FUR_1 | 61 | 65 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.478 |
CLV_PCSK_PC7_1 | 114 | 120 | PF00082 | 0.778 |
CLV_PCSK_PC7_1 | 159 | 165 | PF00082 | 0.421 |
CLV_PCSK_PC7_1 | 223 | 229 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 268 | 274 | PF00082 | 0.426 |
CLV_PCSK_PC7_1 | 50 | 56 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.571 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.598 |
DEG_SPOP_SBC_1 | 504 | 508 | PF00917 | 0.571 |
DOC_CKS1_1 | 302 | 307 | PF01111 | 0.558 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.549 |
DOC_CKS1_1 | 356 | 361 | PF01111 | 0.531 |
DOC_CKS1_1 | 383 | 388 | PF01111 | 0.531 |
DOC_CKS1_1 | 410 | 415 | PF01111 | 0.538 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.568 |
DOC_MAPK_gen_1 | 159 | 168 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 268 | 277 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 50 | 59 | PF00069 | 0.427 |
DOC_SPAK_OSR1_1 | 157 | 161 | PF12202 | 0.419 |
DOC_SPAK_OSR1_1 | 266 | 270 | PF12202 | 0.419 |
DOC_SPAK_OSR1_1 | 48 | 52 | PF12202 | 0.417 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.687 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 148 | 158 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 257 | 267 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 505 | 512 | PF00244 | 0.572 |
LIG_Actin_WH2_2 | 200 | 216 | PF00022 | 0.549 |
LIG_Actin_WH2_2 | 91 | 107 | PF00022 | 0.555 |
LIG_EH_1 | 438 | 442 | PF12763 | 0.498 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.551 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.552 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.486 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.572 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.560 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 436 | 441 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.510 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 255 | 259 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.411 |
LIG_SH3_1 | 100 | 106 | PF00018 | 0.555 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.530 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.546 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.523 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.480 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.551 |
MOD_CDK_SPxxK_3 | 6 | 13 | PF00069 | 0.558 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.731 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.568 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.578 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.416 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.393 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.397 |
MOD_Cter_Amidation | 115 | 118 | PF01082 | 0.570 |
MOD_Cter_Amidation | 224 | 227 | PF01082 | 0.566 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.500 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.488 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.552 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.515 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.389 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.400 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.551 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.565 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.551 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.502 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.576 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.544 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.532 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.552 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.555 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.517 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.493 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.784 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.550 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.549 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.799 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.515 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.549 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.530 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.448 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.571 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.601 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.648 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.482 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.488 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.516 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.554 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.559 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.567 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.533 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.533 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.540 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.569 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.578 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.582 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.801 |
TRG_ER_diArg_1 | 158 | 161 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.468 |
TRG_NLS_Bipartite_1 | 117 | 132 | PF00514 | 0.554 |
TRG_NLS_Bipartite_1 | 226 | 241 | PF00514 | 0.554 |
TRG_NLS_MonoExtC_3 | 127 | 133 | PF00514 | 0.551 |
TRG_NLS_MonoExtC_3 | 18 | 24 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 236 | 242 | PF00514 | 0.770 |
TRG_NLS_MonoExtN_4 | 17 | 23 | PF00514 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 164 | 169 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 273 | 278 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 55 | 60 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4H3G1 | Leishmania braziliensis | 91% | 100% |