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: 3, no: 2 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HGD0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.546 |
CLV_PCSK_FUR_1 | 234 | 238 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.480 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.539 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.658 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.531 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.618 |
DOC_CYCLIN_yCln2_LP_2 | 322 | 328 | PF00134 | 0.709 |
DOC_MAPK_gen_1 | 316 | 322 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 173 | 176 | PF13499 | 0.673 |
DOC_PP2B_LxvP_1 | 322 | 325 | PF13499 | 0.714 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.698 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.577 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 392 | 400 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 471 | 481 | PF00244 | 0.434 |
LIG_APCC_ABBA_1 | 399 | 404 | PF00400 | 0.508 |
LIG_BRCT_BRCA1_1 | 393 | 397 | PF00533 | 0.533 |
LIG_EVH1_2 | 208 | 212 | PF00568 | 0.534 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.697 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.661 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.551 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.630 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.434 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.616 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.553 |
LIG_Integrin_RGD_1 | 96 | 98 | PF01839 | 0.684 |
LIG_LIR_Gen_1 | 394 | 402 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.511 |
LIG_PCNA_PIPBox_1 | 241 | 250 | PF02747 | 0.590 |
LIG_PCNA_yPIPBox_3 | 234 | 248 | PF02747 | 0.592 |
LIG_PDZ_Class_3 | 476 | 481 | PF00595 | 0.548 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.437 |
LIG_SH2_SRC | 20 | 23 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.486 |
LIG_SH3_2 | 208 | 213 | PF14604 | 0.539 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.548 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.648 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.675 |
LIG_SUMO_SIM_par_1 | 434 | 439 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 83 | 88 | PF11976 | 0.540 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.597 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.701 |
LIG_TRFH_1 | 397 | 401 | PF08558 | 0.520 |
LIG_TYR_ITIM | 462 | 467 | PF00017 | 0.481 |
LIG_WRC_WIRS_1 | 408 | 413 | PF05994 | 0.493 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.537 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.688 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.647 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.679 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.593 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.513 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.672 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.576 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.614 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.680 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.690 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.612 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.716 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.592 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.556 |
MOD_Cter_Amidation | 234 | 237 | PF01082 | 0.546 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.674 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.646 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.661 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.596 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.566 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.618 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.633 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.573 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.547 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.534 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.487 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.512 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.615 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.649 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.605 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.669 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.650 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.639 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.562 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.608 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.659 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.647 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.616 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.646 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.596 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.510 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.566 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.641 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.553 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.484 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.490 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.565 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.707 |
MOD_LATS_1 | 187 | 193 | PF00433 | 0.530 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.519 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.705 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.526 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.575 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.519 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.397 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.636 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.626 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.541 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.560 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.583 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.606 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.539 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.482 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.677 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.679 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.680 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.683 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.674 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.561 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.624 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.647 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.527 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.686 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.630 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.578 |
MOD_SUMO_for_1 | 376 | 379 | PF00179 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.698 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.703 |
TRG_NES_CRM1_1 | 444 | 458 | PF08389 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 246 | 251 | PF00026 | 0.668 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IER7 | Leishmania donovani | 57% | 95% |
A4I3G3 | Leishmania infantum | 57% | 95% |
E9AZQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 99% |
Q4Q8I1 | Leishmania major | 57% | 100% |