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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H412
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.723 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.660 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.626 |
DEG_SPOP_SBC_1 | 177 | 181 | PF00917 | 0.587 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.569 |
DOC_ANK_TNKS_1 | 65 | 72 | PF00023 | 0.537 |
DOC_CKS1_1 | 245 | 250 | PF01111 | 0.587 |
DOC_CKS1_1 | 74 | 79 | PF01111 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 106 | 109 | PF00134 | 0.677 |
DOC_MAPK_DCC_7 | 102 | 112 | PF00069 | 0.643 |
DOC_MAPK_DCC_7 | 357 | 365 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 357 | 365 | PF00069 | 0.539 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.653 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.552 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.485 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.594 |
LIG_APCC_ABBAyCdc20_2 | 10 | 16 | PF00400 | 0.485 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_CaM_NSCaTE_8 | 421 | 428 | PF13499 | 0.501 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.429 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.692 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.556 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.632 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.679 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.572 |
LIG_LIR_Apic_2 | 414 | 419 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.632 |
LIG_Pex14_1 | 7 | 11 | PF04695 | 0.501 |
LIG_SH2_PTP2 | 74 | 77 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.491 |
LIG_SH3_2 | 297 | 302 | PF14604 | 0.560 |
LIG_SH3_2 | 55 | 60 | PF14604 | 0.707 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.545 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.589 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.475 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.777 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.609 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.700 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.455 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.573 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.704 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.700 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.721 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.539 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.646 |
LIG_SUMO_SIM_par_1 | 108 | 114 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 368 | 374 | PF11976 | 0.472 |
MOD_CDC14_SPxK_1 | 299 | 302 | PF00782 | 0.563 |
MOD_CDK_SPxK_1 | 296 | 302 | PF00069 | 0.559 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.632 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.660 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.722 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.516 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.623 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.660 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.550 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.522 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.607 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.728 |
MOD_GlcNHglycan | 403 | 407 | PF01048 | 0.599 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.549 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.499 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.633 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.537 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.704 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.567 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.640 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.537 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.708 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.723 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.613 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.496 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.535 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.677 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.547 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.602 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.684 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.425 |
MOD_Plk_2-3 | 368 | 374 | PF00069 | 0.550 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.624 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.498 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.554 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.731 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.632 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.642 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.699 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.573 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.828 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.574 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.575 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.591 |
MOD_SUMO_rev_2 | 381 | 390 | PF00179 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 182 | 187 | PF01217 | 0.557 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0B3 | Leptomonas seymouri | 31% | 100% |
A0A3S5H5D9 | Leishmania donovani | 63% | 93% |
A4HS95 | Leishmania infantum | 63% | 93% |
E9ACP9 | Leishmania major | 62% | 100% |
E9AK79 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 96% |